Canonical Allele Identifier: CA2683986476

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99769786-T-TTGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769789_99769792dup , CM000669.2:g.99769789_99769792dup	GRCh38
NC_000007.13:g.99367412_99367415dup , CM000669.1:g.99367412_99367415dup	GRCh37
NC_000007.12:g.99205348_99205351dup	NCBI36
NG_008421.1:g.19396_19399dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.499_502dup	ENSP00000337915.3:p.Lys168ArgfsTer20
ENST00000651514.1:c.499_502dup MANE Select	ENSP00000498939.1:p.Lys168ArgfsTer20
ENST00000651783.1:c.58-1283_58-1280dup	ENSP00000498924.1:n.58-1283_58-1280dup
ENST00000652018.1:c.352_355dup	ENSP00000498733.1:p.Lys119ArgfsTer20
ENST00000336411.6:c.499_502dup	ENSP00000337915.2:p.Lys168ArgfsTer20
ENST00000354593.6:c.72-1288_72-1285dup	ENSP00000346607.2:n.72-1288_72-1285dup
ENST00000480043.1:n.396_399dup
NM_001202855.2:c.499_502dup	NP_001189784.1:p.Lys168ArgfsTer20
NM_017460.5:c.499_502dup	NP_059488.2:p.Lys168ArgfsTer20
XM_011515841.1:c.499_502dup	XP_011514143.1:p.Lys168ArgfsTer20
XM_011515842.1:c.499_502dup	XP_011514144.1:p.Lys168ArgfsTer20
NM_017460.6:c.499_502dup MANE Select	NP_059488.2:p.Lys168ArgfsTer20
NM_001202855.3:c.499_502dup	NP_001189784.1:p.Lys168ArgfsTer20